Diclofenac Sodium Gel
Product Images NDC 71085-084

3 FDA label images from Ipg Pharmaceuticals, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 71085-084). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ipg Pharmaceuticals, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Image Description (Example Image)

Image Description (Example Image)
An instructional diagram showing application sites for diclofenac sodium topical gel. Illustrations indicate the upper body (hand, elbow, wrist), lower body (knee and ankle), and specific reference to left and right knees as appropriate areas for gel application.*
FDA Label Image

Image Description (Label1)

Image Description (Label1)
Packaging label for Diclofenac Sodium topical gel 1% (10 mg/g) by IPG Pharmaceuticals, Inc. The label includes Drug Facts, usage instructions, warnings, and treatment areas such as hand, wrist, elbow, foot, ankle, and knee. The net weight is 110 g. The label stresses topical use only and provides detailed safety and dosing information.*
FDA Label Image

Image Description (Label2)

Image Description (Label2)
Label for Diclofenac Sodium Topical Gel, 1%, an arthritis pain reliever NSAID in a 110-gram tube. The label includes warnings about allergic reactions, liver and stomach bleeding risks, and instructions for use and storage. It is manufactured by IPG Pharmaceuticals, Inc. in Phoenix, AZ, and stresses keeping the product out of reach of children.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.